galaxyproject / galaxy-beta1Links
Galaxy Github repository BETA 1. May be destroyed and recreated if post-conversion problems are found (but post-conversion commits on this repo will be reapplied to any recreations). Scary disclaimer aside, so far so good! Full details:
☆12Updated 10 years ago
Alternatives and similar repositories for galaxy-beta1
Users that are interested in galaxy-beta1 are comparing it to the libraries listed below
Sorting:
- ☆12Updated 3 years ago
- An easy-to-use way for running Galaxy workflows.☆20Updated 5 years ago
- prioritize effects of variant annotations from VEP, SnpEff, et al.☆34Updated 6 months ago
- FLS Galaxy tools and tool-wrappers for in-house and third-party bioinformatic applications.☆14Updated last year
- Simon's Data Club - Reference data for Galaxy servers☆10Updated last year
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆50Updated 6 months ago
- Stupid Simple Structural Variant View☆25Updated 8 years ago
- Open-source opinionated Galaxy-based framework for microbiota analysis☆14Updated 4 years ago
- cache packages permanently☆14Updated 11 months ago
- ☆37Updated 4 years ago
- BreakSeq2: Ultrafast and accurate nucleotide-resolution analysis of structural variants☆24Updated 9 years ago
- Precursor to SnakeChunks, see https://github.com/SnakeChunks/SnakeChunks. This project has moved and will no longer be edited here.☆11Updated 7 years ago
- ☆13Updated 7 years ago
- What's The Function of these genes?☆22Updated 8 years ago
- Turn Galaxy Workflows into standalone scripts.☆9Updated 2 years ago
- CheckQC inspects the content of an Illumina runfolder and determines if it passes a set of quality criteria☆28Updated 2 weeks ago
- A tool for Read Multi-Mapper Resolution☆23Updated 8 years ago
- An algorithm for clonal tree reconstruction from multi-sample cancer sequencing data☆14Updated 7 years ago
- Tools for next-generation sequencing analysis☆88Updated 6 years ago
- Import a CWL workflow specification to Nextflow script (experimental)☆27Updated 6 years ago
- Toil workflows for common genomic pipelines☆33Updated 5 years ago
- Simplify snpEff annotations for interesting cases☆22Updated 6 years ago
- Import and run CWL workflows on DNAnexus (alpha)☆13Updated 6 years ago
- SMBL - SnakeMake Bioinformatics Library. Automatic installation of bioinformatics software in your SnakeMake pipelines.☆23Updated 7 years ago
- Tools for generating and decoding error-correcting DNA barcodes☆16Updated 3 years ago
- Collection of galaxy tools developed by the artbio-platform at the IBPS (Institut de Biologie Paris-Seine)☆13Updated 3 months ago
- Preprocessing tools for unique molecular index (UMI) sequencing reads☆31Updated 2 years ago
- vcf file manipulation☆21Updated 9 years ago
- Trigger the Google Genomics Pipeline API with CWL☆11Updated 8 years ago
- Nextflow workshop 2018 -- Training pages -> https://nextflow-io.github.io/nf-hack18/☆18Updated 6 years ago